Job Description
Do you want to be part of our General Medicines, Vaccines and Infectious Diseases (GenMed-VID) team and help bringing new medical advancements to patients?
We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. We have a new, exciting opportunity for a Regulatory Affairs Associate Liaison to be based in Brussels (BE), Oss (NL) or London (UK).
As an Associate Liaison, you will provide procedural, administrative, and planning support for new marketing authorization applications and variation submissions in the EU, UK, Switzerland, and non-EU South Eastern European countries (non-EU SEE) under supervision from the (Senior) Principal Scientist of Regulatory Affairs. You will work on products approved through Centralized and Decentralized/MRP procedures, collaborating with the (Senior) Principal Scientist and cross-functional teams.
Our department
Regulatory Affairs Europe is part of Global Regulatory Affairs and Clinical Safety (GRACS). In GRACS we are always striving for operational excellence. We cover a wide range of activities related to getting products and keeping them on the market. The health authority is our most important stakeholder; our end goal is to ensure innovative medicines reach patients. Our large portfolio in GenMed-VID includes medicinal products at all stages of the marketing authorization’s life cycle and span several therapeutic indications. Activities are numerous and the dedication and commitment of the team is very rewarding. Our portfolio provides the chance to learn something new every day!
What You’ll Do
Administrative support: Provides administrative support during filling and review of new product registrations and post-approval submissions (variations, CHMP referrals, Agency commitments etc.) in the EU and the UK, Switzerland, and non-EU SEE countries
Coordinate submissions: Plan and coordinate regulatory submissions to ensure timely delivery.
Prepare Module 1: Draft and organize regional administrative documents and liaise with internal teams for completeness and accuracy.
Collaborate cross-functionally: Work closely with Regulatory Operations and Country RA Managers to establish submission timelines and align on submission strategy and execution.
Manage translations: For centralized procedures, oversee translation processes to meet EMA requirements.
Artwork development: Coordinates new product artwork development and/or artwork updates implementation.
Maintain compliance: Keep regulatory databases updated and ensure adherence to EU legislation and procedural requirements.
Contribute to projects: Act as a subject matter expert in workstreams and process improvement initiatives.
What We’re Looking For
University degree in life sciences or related field.
Up to 5 years of experience in the pharmaceutical industry with knowledge of drug development and approval processes.
Strong organizational and project management abilities with the ability to manage multiple tasks and to prioritize them efficiently.
Excellent written and verbal communication in English.
Familiarity with EU regulatory procedures (CP, DCP, MRP) and Module 1 requirements.
Ability to work in an international environment and coordinate multiple stakeholders.
Detail-oriented with strong document review and QC skills.
Proactive, solution-oriented, and eager to contribute to process improvements.
Experience with AI-enabled tools (e.g. for document management, data review, process efficiency, or knowledge retrieval)
Willingness to travel up to 5% for job-related activities.
Required Skills:
Accountability, Adaptability, Audits Compliance, Detail-Oriented, EU Pharmaceutical Regulations, Communication, Pharmacovigilance, Process Improvements, Project Management, Regulatory Compliance, Regulatory Operations, Regulatory Strategy Development, Regulatory Submissions, Digital & AI literacy (use of AI-enabled tools to support regulatory, administrative, and process-improvement activities).
Required Skills:
Adaptability, Audits Compliance, Cross-Functional Collaboration, Detail-Oriented, Drug Development, Drug Regulatory Affairs, Employee Training Programs, EU Regulations, Foreign Policy, Global Communications, On Time Deliveries, Pharmaceutical Development, Pharmaceutical Regulatory Affairs, Pharmacovigilance, Process Improvements, Product Approvals, Project Management, Public Administration, Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory Compliance, Regulatory Operations, Regulatory Strategy Development, Regulatory Submissions, Translation Management
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Hybrid
Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
06/16/2026
- A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID:R396450
